Mutation

Primary Site >> Stomach Cancer

Gene >> CACNA1G

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50572003:50572003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.712C>T
AA Mutation	p.Arg238Trp(p.R238W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50603102:50603102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776132057
CDS Mutation	c.4072G>A
AA Mutation	p.Val1358Ile(p.V1358I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50615465:50615465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4864G>A
AA Mutation	p.Gly1622Arg(p.G1622R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50626099:50626099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201791887
CDS Mutation	c.6482C>T
AA Mutation	p.Pro2161Leu(p.P2161L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50603181:50603181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4151G>A
AA Mutation	p.Arg1384Gln(p.R1384Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50599596:50599596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3427G>A
AA Mutation	p.Glu1143Lys(p.E1143K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50578397:50578397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781006063
CDS Mutation	c.2134C>T
AA Mutation	p.Arg712Trp(p.R712W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50576237:50576237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1835C>T
AA Mutation	p.Ala612Val(p.A612V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50606978:50606978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4501G>A
AA Mutation	p.Val1501Met(p.V1501M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50616365:50616365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5002C>T
AA Mutation	p.Arg1668Cys(p.R1668C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50591499:50591499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2518C>T
AA Mutation	p.Arg840Cys(p.R840C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50602823:50602823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3919C>T
AA Mutation	p.Arg1307Cys(p.R1307C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50569270:50569270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762860094
CDS Mutation	c.460C>T
AA Mutation	p.Arg154Trp(p.R154W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50618260:50618260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5344C>T
AA Mutation	p.His1782Tyr(p.H1782Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50615366:50615366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4765C>A
AA Mutation	p.Gln1589Lys(p.Q1589K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50578473:50578473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537429256
CDS Mutation	c.2210G>A
AA Mutation	p.Arg737Gln(p.R737Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50572660:50572660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.853G>A
AA Mutation	p.Val285Met(p.V285M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50618686:50618686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5459C>T
AA Mutation	p.Thr1820Ile(p.T1820I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50626339:50626339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6722G>A
AA Mutation	p.Arg2241Gln(p.R2241Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50603048:50603048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4018G>A
AA Mutation	p.Ala1340Thr(p.A1340T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000359106
Start	50606901:50606901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4424C>G
AA Mutation	p.Ala1475Gly(p.A1475G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000359106
Start	50624057:50624057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6211C>A
AA Mutation	p.Leu2071Ile(p.L2071I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359106
Start	50596794:50596794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766326181
CDS Mutation	c.3129G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359106
Start	50618963:50618963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5736G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359106
Start	50602858:50602858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3954C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359106
Start	50626409:50626409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781152093
CDS Mutation	c.6792G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359106
Start	50600749:50600749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755158469
CDS Mutation	c.3714G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359106
Start	50626559:50626559(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.6948delC
AA Mutation	p.Glu2317ArgfsTer47(p.E2317Rfs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359106
Start	50626658:50626658(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.7046delC
AA Mutation	p.Pro2349LeufsTer15(p.P2349Lfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000359106
Start	50575698:50575698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1296C>A
AA Mutation	p.Cys432Ter(p.C432*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000359106
Start	50604282:50604282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4296+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript